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石蒜科生物碱属于不同结构亚组,对抗细胞凋亡的癌细胞具有活性。

Amaryllidaceae alkaloids belonging to different structural subgroups display activity against apoptosis-resistant cancer cells.

机构信息

Laboratoire de Toxicologie and Laboratoire de Chimie Analytique, Toxicologie et Chimie Physique Appliquee, Institut de Pharmacie, Universite Libre de Bruxelles, Brussels, Belgium.

出版信息

J Nat Prod. 2010 Jul 23;73(7):1223-7. doi: 10.1021/np9008255.

Abstract

Fifteen Amaryllidaceae alkaloids (1-15) were evaluated for their antiproliferative activities against six distinct cancer cell lines. Several of these natural products were found to have low micromolar antiproliferative potencies. The log P values of these compounds did not influence their observed activity. When active, the compounds displayed cytostatic, not cytotoxic activity, with the exception of pseudolycorine (3), which exhibited cytotoxic profiles. The active compounds showed similar efficacies toward cancer cells irrespective of whether the cell lines were responsive or resistant to proapoptotic stimuli. Altogether, the data from the present study revealed that lycorine (1), amarbellisine (6), haemanthamine (14), and haemanthidine (15) are potentially useful chemical scaffolds to generate further compounds to combat cancers associated with poor prognoses, especially those naturally resistant to apoptosis, such as glioblastoma, melanoma, non-small-cell lung, and metastatic cancers.

摘要

15 种石蒜科生物碱(1-15)被评估了其对六种不同癌细胞系的抗增殖活性。这些天然产物中的几种被发现具有低微摩尔的抗增殖效力。这些化合物的 log P 值并不影响其观察到的活性。当具有活性时,化合物表现出细胞生长抑制剂,而不是细胞毒性活性,除了伪石蒜碱(3),其表现出细胞毒性特征。活性化合物显示出对癌细胞的相似功效,无论细胞系是否对促凋亡刺激敏感或耐药。总的来说,本研究的数据表明,石蒜碱(1)、石蒜宁(6)、海曼胺(14)和海曼定(15)是潜在有用的化学支架,可以生成进一步的化合物来对抗与预后不良相关的癌症,特别是那些天然对细胞凋亡耐药的癌症,如神经胶质瘤、黑色素瘤、非小细胞肺癌和转移性癌症。

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